Enhanced antifungal activity of sugarcane cv. NCo310 expressing chimeric chitinase 42

The development of sustainable and environmentally safe strategies for crop protection against fungal pathogens is a significant challenge in agriculture. This paper discusses the successful transfer of a chimeric chitinase 42 gene into sugarcane using the biolistic method, resulting in an enhanced antifungal activity. Chitinases possess the enzymatic capability to degrade chitin, a key component of the cell walls in various fungal phytopathogens. In this research, we employed a chimeric chitinase 42 that combines the 42 kDa chitinase from Trichoderma atroviridae with a chitin binding domain from Serratia marcescens chitinase B. This chimeric chitinase exhibits higher antifungal activity against phytopathogenic fungi. PCR analysis confirmed the integration of the transgene into the genome of transformants, while the expression of the transgene was assessed using reverse transcription-PCR. Transgenic lines showed to have different chitinase activity and a high increase in chitinase activity was detected in lines T3, T5 and T6 with about 18 U/mg chitinase activity compared to the control plants (2.8 U/mg). Antifungal activity of transgenic lines T3, T5 and T6 on sugarcane fungal pathogens was shown in radial diffusion and detached leaf assays. The enhanced antifungal activity observed in the transformed sugarcane lines indicates the potential of chimeric chitinase 42 as an effective antifungal agent. •Transformation of chimeric chitinase gene containing chitin binding domain into sugarcane to tackle major fungal diseases•Successful application of particle bombardment towards obtaining transgenic sugarcane as a recalcitrant plant.•Challenging obtained transgenic lines against a diverse group of sugarcane pathogenic fungi•The use of NCo310 variety of sugarcane as a dominant variety cultivated in the southern regions of Iran.